GOLD

N/A

79,992 FDA adverse event reports analyzed

Last updated: 2026-04-15

About GOLD

GOLD is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for GOLD include DRUG INEFFECTIVE, RHEUMATOID ARTHRITIS, DRUG INTOLERANCE, JOINT SWELLING, OFF LABEL USE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for GOLD.

Top Adverse Reactions

DRUG INEFFECTIVE3,429 reports
RHEUMATOID ARTHRITIS2,742 reports
DRUG INTOLERANCE1,985 reports
JOINT SWELLING1,948 reports
OFF LABEL USE1,908 reports
ARTHRALGIA1,818 reports
DRUG HYPERSENSITIVITY1,817 reports
ARTHROPATHY1,720 reports
PAIN1,598 reports
CONDITION AGGRAVATED1,524 reports
TREATMENT FAILURE1,510 reports
CONTRAINDICATED PRODUCT ADMINISTERED1,454 reports
NAUSEA1,282 reports
RASH1,258 reports
THERAPEUTIC PRODUCT EFFECT DECREASED1,177 reports
HEADACHE1,162 reports
ABDOMINAL DISCOMFORT1,122 reports
DIARRHOEA1,063 reports
MUSCULOSKELETAL STIFFNESS1,063 reports
FATIGUE1,059 reports
PERIPHERAL SWELLING1,038 reports
HYPERTENSION1,011 reports
SYNOVITIS991 reports
MALAISE960 reports
C REACTIVE PROTEIN INCREASED907 reports
MOBILITY DECREASED906 reports
HAND DEFORMITY882 reports
INFLAMMATION862 reports
VOMITING858 reports
PAIN IN EXTREMITY837 reports
SWELLING833 reports
INFECTION831 reports
HYPERSENSITIVITY798 reports
DIZZINESS793 reports
HEPATIC ENZYME INCREASED739 reports
PRODUCT USE ISSUE739 reports
PSORIATIC ARTHROPATHY738 reports
ALOPECIA736 reports
C REACTIVE PROTEIN ABNORMAL721 reports
PNEUMONIA710 reports
MUSCULOSKELETAL PAIN705 reports
GASTROINTESTINAL DISORDER684 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE678 reports
INTENTIONAL PRODUCT USE ISSUE667 reports
INSOMNIA660 reports
FIBROMYALGIA657 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE656 reports
INFUSION RELATED REACTION642 reports
STOMATITIS642 reports
URTICARIA636 reports
ABDOMINAL PAIN UPPER634 reports
GENERAL PHYSICAL HEALTH DETERIORATION620 reports
GLOSSODYNIA610 reports
BLOOD CHOLESTEROL INCREASED609 reports
RED BLOOD CELL SEDIMENTATION RATE INCREASED587 reports
OSTEOARTHRITIS577 reports
JOINT RANGE OF MOTION DECREASED567 reports
LOWER RESPIRATORY TRACT INFECTION566 reports
HYPOAESTHESIA527 reports
PEMPHIGUS524 reports
SYSTEMIC LUPUS ERYTHEMATOSUS524 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES523 reports
ASTHENIA519 reports
NASOPHARYNGITIS517 reports
ILL DEFINED DISORDER515 reports
SLEEP DISORDER500 reports
ARTHRITIS496 reports
NAIL DISORDER494 reports
FOLLICULITIS484 reports
HELICOBACTER INFECTION482 reports
WEIGHT INCREASED473 reports
BURSITIS468 reports
MATERNAL EXPOSURE DURING PREGNANCY468 reports
GRIP STRENGTH DECREASED466 reports
DYSPNOEA456 reports
BREAST CANCER STAGE III454 reports
DEPRESSION448 reports
DUODENAL ULCER PERFORATION448 reports
CONFUSIONAL STATE446 reports
PERICARDITIS444 reports
LUNG DISORDER437 reports
MEMORY IMPAIRMENT436 reports
RHEUMATOID FACTOR POSITIVE436 reports
MUSCULAR WEAKNESS434 reports
OBESITY434 reports
BLISTER433 reports
LIVER FUNCTION TEST INCREASED429 reports
DECREASED APPETITE426 reports
IMPAIRED HEALING422 reports
PRODUCT USE IN UNAPPROVED INDICATION421 reports
IRRITABLE BOWEL SYNDROME418 reports
GASTROOESOPHAGEAL REFLUX DISEASE417 reports
HYPERCHOLESTEROLAEMIA415 reports
ABDOMINAL PAIN410 reports
FACET JOINT SYNDROME410 reports
DRY MOUTH409 reports
DRUG INDUCED LIVER INJURY404 reports
MUSCLE SPASMS402 reports
PULMONARY FIBROSIS399 reports
ADVERSE REACTION398 reports

Frequently Asked Questions

How many FDA adverse event reports are associated with GOLD?

This profile reflects 79,992 FDA FAERS reports that mention GOLD. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for GOLD?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, RHEUMATOID ARTHRITIS, DRUG INTOLERANCE, JOINT SWELLING, OFF LABEL USE, ARTHRALGIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.